Symbiont infection and psyllid haplotype influence phenotypic plasticity during host switching events

Many herbivorous insect species exhibit phenotypic plasticity when using multiple hosts, which facilitates survival in heterogeneous host environments. Physiological host acclimation is an important part of it, yet the effects of host acclimation on insect feeding behaviour are not well studied, par...

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Veröffentlicht in:Ecological entomology 2024-10, Vol.49 (5), p.719-733
Hauptverfasser: Gebiola, Marco, Mauck, Kerry E.
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Sprache:eng
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Zusammenfassung:Many herbivorous insect species exhibit phenotypic plasticity when using multiple hosts, which facilitates survival in heterogeneous host environments. Physiological host acclimation is an important part of it, yet the effects of host acclimation on insect feeding behaviour are not well studied, particularly for insect vectors of plant pathogens. We studied the combined effects of host acclimation and infection with a plant pathogenic symbiont on feeding behaviour of Bactericera cockerelli, an oligophagous psyllid widespread in both crop and natural habitats that feed primarily on Solanaceae and transmit an economically important plant pathogen, Candidatus Liberibacter solanacearum (CLso). We used a factorial design and the electrical penetration graphing technique to disentangle the effects of host acclimation, CLso infection and psyllid haplotype on the within‐plant feeding behaviour of B. cockerelli during conspecific and heterospecific host switches. This approach allows to connect phenotypic plasticity with the role of B. cockerelli as a vector by quantifying the frequency and duration of behaviours involved in CLso transmission. We found significant reductions in multiple metrics of B. cockerelli feeding efficiency, exacerbated by infection with CLso, which could lead to reduced transmission of this pathogen. Psyllid genotype was also important; the Central haplotype exhibited less dramatic changes in feeding efficiency than the Western haplotype during heterospecific host switches. Our study shows that host acclimation and heterospecific host switching directly alter feeding behaviours underlying pathogen transmission, and that the magnitude of feeding efficiency reductions depends on both host genotype and infection status. Host acclimation and heterospecific host switching directly alter feeding behaviours of the potato psyllid Bactericera cockerelli underlying pathogen transmission Reduction in feeding efficiency is exacerbated by psyllid infection with the plant pathogen Candidatus Liberibacter solanacearum Psyllid genotype is also an important factor, as the Central haplotype exhibited less dramatic changes in feeding efficiency than the Western haplotype
ISSN:0307-6946
1365-2311
DOI:10.1111/een.13342